SNP Report

Basic Info

Name	rs9616217 dbSNP Ensembl
Location	chr22:49925298 - 49925298(1)
Variant Alleles	C/T
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.295927
Functional Annotation	downstream_gene_variant; intron_variant; non_coding_transcript_exon_variant; non_coding_transcript_variant.
Consequence to Transcript	downstream_gene_variant(ENST00000444954, ENST00000450207, ENST00000462253, ENST00000482956, ENST00000498354); intron_variant(ENST00000328268, ENST00000403427, ENST00000404488, ENST00000407217, ENST00000483652); non_coding_transcript_exon_variant(ENST00000487969); non_coding_transcript_variant(ENST00000483652, ENST00000487969)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
CRELD2	cysteine-rich with EGF-like domains 2	22q13.33	Mapped by LD-proxy

SNPs in LD with rs9616217 (count: 0) View in gBrowse (chr22:49925298..49925298 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)